Description

Many of the world’s 6,000 to 8,000 rare diseases are chronic, progressive, and often life-threatening, but few can be treated effectively—or even diagnosed reliably and early enough for best therapeutic outcomes. The International Rare Diseases Research Consortium (IRDiRC), launched in 2011 by the European Commission and the U.S. National Institutes of Health, unites public and private funders and coordinates research efforts toward an ambitious goal: develop 200 new therapies and means to diagnose most rare diseases by 2020.

Learning Objectives:

  • Describe how IRDiRC and its partner organizations operate in an international arena
  • Attract interested organizations (pharmaceutical, diagnostics companies, and research investors)
  • Present the opportunities and challenges of developing drugs and diagnostics for rare diseases

Ability Level: All

Session ID: 2003

Speakers (3)

contact_4370 Luc Dochez Chief Business Officer Prosensa
contact_8649 Pamela Gavin Chief Operating Officer National Organization for Rare Disorders, Inc.
contact_9920 Lu Wang Program Director National Human Genome Research Institute

Moderators (1)

contact_4632 Ruxandra Draghia-Akli Director, Health Research European Commission